Construction of super-hydrophobic hypercrosslinked porous polymers for selectively removing aromatic diamines from the polyurethane bio-hydrolysate

被引:20
作者
Chen, Liyan [1 ,2 ]
Rong, Meng [1 ]
Yang, Liangrong [1 ,2 ,3 ]
Yu, Jiemiao [1 ]
Qu, Hongnan [1 ]
Meng, Qiyu [1 ]
Ni, Shan [1 ,2 ]
Xu, Zihao [1 ,2 ]
Zhu, Xiangyang [1 ,2 ]
Wang, Li [1 ]
Xing, Huifang [1 ,2 ,3 ]
Liu, Huizhou [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Inst Proc Engn, State Key Lab Biochem Engn, CAS Key Lab Green Proc & Engn, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Engn, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, CAS Key Lab Biobased Mat, Qingdao 266101, Peoples R China
基金
中国国家自然科学基金; 欧盟地平线“2020”;
关键词
Selective adsorption; Super-hydrophobicity; Hypercrosslinked polymers; Aromatic diamines; Polyurethane hydrolysate; MICROPOROUS POLYMERS; BIODEGRADATION; ADSORPTION; BACTERIUM; PURIFICATION; SEPARATION; RECOVERY; INSIGHTS; DEGRADES; ENZYME;
D O I
10.1016/j.cej.2021.132509
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The upcycling of Polyurethane (PU) degradation products has been gaining tremendous attention and research interest in recent years. In particular, due to the toxicity to microorganisms, the key process is to remove aromatic diamines selectively and efficiently from the bio-hydrolysate which also includes multiple carboxylic di acids and polyols. Herein, a series of super-hydrophobic hypercrosslinked porous polymers (HCPPs) were prepared to selectively remove aromatic diamines in a neutral condition. They were facially fabricated via Friedel-Crafts alkylation reactions with benzene and three types of benzyl bromides. Besides, the surface area, porous structure, and hydrophobic properties of resulting polymers were adjusted by changing the length and connected nodes numbers of crosslinkers. Particularly, HCPP-TBMB knitted by 1,3,5-tris(bromomethyl)-benzene (TBMB) owned a maximum BET surface area of 1048.8 m(2) g(-1) with hierarchical porosity, as well as high thermal stability and super-hydrophobicity. The adsorption experiments on HCPP-TBMB clarified the large adsorption capacities of 2,4-toluene diamine (TDA, 1.062 mmol g-1) and 4,4'-methylene dianiline (MDA, 1.971 mmol g-1) as well as high selectivity in the model PU hydrolysate. Moreover, thermodynamic experiments and spectral analysis revealed the physical adsorption process for uptake of aromatic diamines on HCPP-TBMB. The main adsorption mechanism contained 7C-7C stacking, hydrophobic interaction, and hole size effect. These findings may provide a promising strategy for highly selective removal of aromatic diamines from the PU bio-hydrolysate.
引用
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页数:12
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